Lozar-Krivec Jana, Stepic Maja, Hovnik Tinka, Krsnik Mladen, Paro-Panjan Darja
*Department of Neonatology, Division of Paediatrics †Division of Paediatrics, Centre for Medical Genetics ‡Institute of Clinical Chemistry and Biochemistry, University Medical Centre Ljubljana, Slovenia.
J Pediatr Hematol Oncol. 2016 Oct;38(7):e267-70. doi: 10.1097/MPH.0000000000000655.
Neonatal cyanosis is rarely due to hemoglobin variants with low oxygen affinity. We describe the clinical course and results of molecular genetic analysis of a boy who presented after birth with severe cyanosis. Arterial blood-gas analysis demonstrated a pronounced shift of the oxygen-hemoglobin dissociation curve to the right and molecular genetic analysis revealed a γ-globin variant, Hb F-Sarajevo. The patient presented is the second reported case of neonatal cyanosis due to this mutation, which was first described in 2012 by Zimmermann-Baer and coauthors. With the introduction of universal screening for congenital heart disease, the finding of low oxygen saturation will uncover more neonates with hemoglobinopathies with low oxygen affinity.
新生儿发绀很少由具有低氧亲和力的血红蛋白变异体引起。我们描述了一名出生后出现严重发绀的男孩的临床过程和分子遗传学分析结果。动脉血气分析显示氧合血红蛋白解离曲线明显右移,分子遗传学分析揭示了一种γ-珠蛋白变异体,即Hb F-萨拉热窝。本文报道的患者是该突变导致新生儿发绀的第二例病例,该突变于2012年由齐默尔曼-拜尔及其合著者首次描述。随着先天性心脏病普遍筛查的引入,低氧饱和度的发现将揭示更多患有低氧亲和力血红蛋白病的新生儿。